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Webinar: How Biosimilar Rebates Shape Payer Policies, Provider Behavior
An upcoming webinar from MJH Life Sciences™ will address the payer rebate deals that limit provider choice of biosimilars and complicate clinical pharmacy operations.
More biosimilars are being launched, but numerous factors affect whether they become available in the clinic. On Monday, July 20, 2020, from 5 to 6 pm EST, MJH Life Sciences™ is hosting a webinar about how biosimilar rebates shape payer policies and provider options.
The program features a panel of leading experts on oncology practice and payment who will provide perspectives on how the structuring of biosimilar payment contracts at the payer level is affecting biosimilar access and cost at the provider level.
With more biosimilars, the expectation is that costs will decline and providers will have more freedom to choose the most appropriate medications for their patients. However, marketplace dynamics have made that ideal a more complicated objective than anticipated.
Providers who want to use biosimilars find their choices of these medicines often are determined not by clinical concerns but by regional payer-by-payer contracts that necessitate careful pharmacy planning, staff training, and sometimes, compromise.
Hear what our panelists have to say about these issues and how they deal with them. They are Kathy W. Oubre, MS, chief operating officer of the Pontchartrain Cancer Center in Louisiana; Ali McBride, PharmD, MS, BCOP, FASHP, FAzPA, clinical coordinator of Hematology/Oncology for The University of Arizona Cancer Center; and Timothy Chiu, PharmD, BCPS, pharmacist evidence analyst and strategist for Kaiser Permanente.
Click here for registration information.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Eye on Pharma: EU Aflibercept Approvals; Biosimilars Canada Campaign; Celltrion Data
November 19th 2024The European Commission grants marketing authorization to 2 aflibercept biosimilars; Biosimilars Canada launches new campaign to provide sustainable solutions to employers; Celltrion shares positive data for 2 biosimilars.
Can Global Policies to Boost Biosimilar Adoption Work in the US?
November 17th 2024On this special episode of Not So Different honoring Global Biosimilars Week, Craig Burton, executive director of the Biosimilars Council, explores how global policies—from incentives to health equity strategies—could boost biosimilar adoption in the US.
Subcutaneous Infliximab CT-P13 Superior to Placebo as Maintenance Therapy for IBD
November 16th 2024In 2 randomized controlled trials of maintenance therapy for inflammatory bowel disease (IBD), the subcutaneous formulation of the infliximab biosimilar CT-P13 demonstrated superiority to placebo in patients with Crohn disease and ulcerative colitis.
